FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

FAICO Dental Implant System and CAD/CAM Abutments

K Number: K211871 · Decision Nov 18, 2021
Classifications
1
FEI Numbers
382
Registration Numbers
382
Same Product Code
708
Applicant Total
3
Review Days
154

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Basic Information

Device Name
FAICO Dental Implant System and CAD/CAM Abutments
K Number
K211871
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3630
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Faico Medical, LLC
Date Received
June 17, 2021
Decision Date
November 18, 2021
Product Code
NHA
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
NHA Abutment, Implant, Dental, Endosseous

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (NHA), ordered by most recent decision date.

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Other Clearances by Faico Medical, LLC

K Number Device Name
K191997 FAICO CMF System
K192015 Faico Dental Implant System